Stanford researchers and their collaborators have revealed a new device that could change the way scientists conduct gene-editing experiments. The device, CRISPR-GPT, is an artificial intelligence lab ...

Scientists developed a new nanostructure that triples CRISPR’s ability to enter cells, unlocking even more power to treat genetic diseases.

As CRISPR continues to drive breakthroughs in medicine, agriculture, and synthetic biology, understanding its origins does more than tell an ancient story. It provides a blueprint for engineering the ...

That’s why a team from UC San Diego in La Jolla set out with Yale University researchers to develop a new system for gene editing that they believe may be safer and more efficient than the common ...

Har Gobind Khorana, a Nobel laureate, deciphered the genetic code, revealing how DNA sequences specify amino acids. His pioneering work in gene synthe ...

Researchers at Duke University used CRISPR technologies to discover previously unannotated stretches of DNA in the "dark genome" that are responsible for controlling how cells sense and respond to the ...

Regulatory T cells help your immune system distinguish between ‘self’ and ‘nonself’ – and can open doors to better treatments for cancer, autoimmune disease and transplant rejection.

This year’s WIRED Health summit in Boston featured Moderna CEO Stéphane Bancel, CNN chief medical correspondent Sanjay Gupta, and a day’s worth of insights and provocative conversations.

The agreement with Algen Biotechnologies gives AstraZeneca exclusive rights to develop and commercialise therapies from the gene-editing technology known as Crispr. Algen was spun out of the Berkeley ...